Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs9657182
IDO1
0.851 0.280 8 39908329 intron variant C/G;T snv 6
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs10881578
RXRA
0.925 0.240 9 134340689 intron variant A/G snv 0.32 2
rs189139
SH3BP2
0.925 0.160 4 2831000 intron variant C/T snv 0.26 2
rs2798224
MSANTD1
1.000 0.120 4 3265941 intron variant G/A snv 0.45 2
rs363092
HTT
1.000 0.120 4 3194302 intron variant A/C;T snv 0.51 2
rs6855981
HTT
1.000 0.120 4 3146549 intron variant G/A snv 0.34 2
rs10015979
HTT
1.000 0.120 4 3107715 intron variant A/G snv 0.30 1
rs10934657
KALRN
1.000 0.120 3 124093989 intron variant T/C snv 0.60 1
rs110501
HTT
1.000 0.120 4 3223751 intron variant T/C snv 0.47 1
rs11248108
RNF4
1.000 0.120 4 2479763 intron variant G/A;T snv 1
rs11731237
HTT
1.000 0.120 4 3150086 intron variant C/T snv 0.26 1
rs1232027
LINC01337
1.000 0.120 5 80619201 intron variant G/A snv 0.32 1
rs13102260
HTT-AS ; HTT
1.000 0.120 4 3074678 intron variant G/A snv 0.15 1
rs1313770
HTT-AS ; HTT
1.000 0.120 4 3056082 intron variant A/G snv 0.57 1
rs1419046
GRK4
1.000 0.120 4 2984322 intron variant T/A snv 0.39 1
rs16844309
RGS12
1.000 0.120 4 3416539 intron variant G/A snv 0.26 1
rs1730768
RGS12
1.000 0.120 4 3407632 intron variant A/G snv 0.85 1
rs2071655
HTT
1.000 0.120 4 3116389 intron variant T/A;G snv 1
rs2269499
HTT
1.000 0.120 4 3237975 intron variant C/T snv 0.24 1
rs2285086
HTT
1.000 0.120 4 3087532 intron variant A/G snv 0.48 1
rs2298969
HTT
1.000 0.120 4 3184517 intron variant A/G;T snv 1